FdaApplication
NDA 020381
Identifiers
- fda_app_no: NDA020381
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 1997-07-28 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NIASPAN | NIACIN | 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
| NIASPAN | NIACIN | 375MG | TABLET, EXTENDED RELEASE;ORAL |
| NIASPAN | NIACIN | 1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
| NIASPAN | NIACIN | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
| NIASPAN TITRATION STARTER PACK | NIACIN | 375MG | TABLET, EXTENDED RELEASE;ORAL |
5 products